FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Laser, Transmyocardial Revascularization

PMA: P970029 · Supplement: S025 · Decision Jan 28, 2014
Classifications
1
FEI Numbers
2
Registration Numbers
2

Basic Information

Device Name
System, Laser, Transmyocardial Revascularization
Trade Name
PEARL 8.0 HANDPIECE
PMA Number
P970029
Supplement Number
S025
Device Class
FDA Class 3
Product Code
MNO
Generic Name
SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
January 28, 2014
Date Received
November 26, 2013
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MNO System, Laser, Transmyocardial Revascularization